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Results for each specimen were classified by probe set into one of six categories.
Bio-CHGC was synthesized, and then its self-assembled nanoparticles were prepared by probe sonication.
The concentrations of the main molecular species have been measured by probe sampling and GC analysis.
Abstract: A method of sequencing nucleic acids by probe hybridization and/or ligation is provided using DNA origami as a barcode for a nucleic acid probe.
The DNA microarray-based results are only valid for a subset of the genome covered by probe sequences on the chip.
Also, bounding boxes enlarged by probe radii larger than 3.0 only include marginally more USR moments.
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As a result of the probe-by-probe normalization method, n and m are not necessarily equal.
Full probe-by-probe results can be found in Table S3.
A linear mixed model analysis was used to identify significant breed-by-probe interactions.
Conclusions: Compatibility between high-density oligonucleotide arrays is significantly affected by probe-level sequence information.
Real-time PCR followed by probe-specific melting-curve analysis allowed differentiation of HPV-6 and HPV-11.
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